Coronary dominance (left or co-dominant vs right dominant)
LINC00840 · rs7083186
1 12237Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others7Total12Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 7,708 European ancestry left or co-dominant individuals, 37,613 European ancestry right dominant individuals.
The effect
Each copy of the C allele carried 0.81 times the odds of Coronary dominance (left or co-dominant vs right dominant) (95% confidence interval 0.77-0.85); p = 1 × 10−16.
How common The C allele had a frequency of about 16% in the people studied.
Where it sits Chromosome 10, band 10q11.21 — in an intron of LINC00840.
What each result means
C/CTwo copies of the version the research linked to Coronary dominance (left or co-dominant vs right dominant). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Coronary dominance (left or co-dominant vs right dominant). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Coronary dominance (left or co-dominant vs right dominant). This is the starting point the study compared everyone against.
rs7083186 is a single position in the genome, in or near the LINC00840 gene. Published research associates it with coronary dominance (left or co-dominant vs right dominant). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7083186 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs7083186 come from?
GWAS Catalog, Cell 2025, PMID:40049164. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 12237Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others7Total12Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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Coronary dominance (left or co-dominant vs right dominant) (rs7083186). MyGeneLog™. https://www.mygenelog.com/variants/rs7083186